34835-57-9

Basic information

• Product Name: Benzenediazonium, 2-bromo-, chloride
• CAS NO: 34835-57-9
• Molecular Formula: C6H4BrN2.Cl
• Molecular Weight: 219.468
• Mol File: 34835-57-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzenediazonium, 2-bromo-, chloride(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenediazonium, 2-bromo-, chloride(34835-57-9)
• EPA Substance Registry System: Benzenediazonium, 2-bromo-, chloride(34835-57-9)

Safety Data

• Hazardous Substances Data: 34835-57-9(Hazardous Substances Data)

Upstream product

• 615-36-1 2-bromoaniline 
• 7647-01-0 hydrogenchloride 
• 64-17-5 ethanol 

Downstream Products

• 46493-66-7 3-phenyl-2,3-dihydro-1,3-benzothiazol-2-imine 
• 1619995-12-8 12-[5-(2-bromophenyl)-1-methyl-1H-pyrrol-2-yl]-9,9-dimethyl-7,8,9,10-tetrahydrobenzo[a]acridin-11(12H)-one 
• 912763-38-3 5-(2-bromophenyl)-1-methyl-1H-pyrrole-2-carbaldehyde 
• 154180-30-0 allyl (2-bromophenyl) thioether 
• 6320-02-1 o-bromothiophenol 
• 935846-34-7 N-methoxy-N-methyl 7-bromo-3-phenyl-1H-indole-2-carboxamide 
• 935846-32-5 ethyl 7-bromo-3-phenylindole-2-carboxylate 

Relevant articles and documents

Preparation of Benzothiophenes by Pd(0)-Catalyzed Intramolecular Cyclization of Allyl (and Propargyl) o-Iodophenyl Sulfides

Benzothiophenes are prepared by intramolecular Pd(0)-catalyzed Heck reaction of allyl o-iodophenyl sulfides.Pd(0)-Catalyzed intramolecular cyclization of o-iodophenyl propargyl sulfide in the presence of a hydride donor gives 3-methylene-2,3-dihydrobenzothiophene, which reacts with several enophiles in ene type reactions.However, allyl (and propargyl) aryl sulfides react with palladium(II) chloride to afford polymeric 2.